Cryptic terminal rearrangement of chromosome 22q13.32 detected by FISH in two unrelated patients.

Author:

Doheny K F,McDermid H E,Harum K,Thomas G H,Raymond G V

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference18 articles.

1. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation;Flint, J.; Wilkie, A.O.M.; Buckle, V.J.; Winter, R.M.; Holland, A.J.; McDermid, H.E.;Nat Genet,1995

2. Clinical, cytogenetic and molecular characterization of seven patients with deletions of chromosome 22q1 3.3;Nesslinger, N.J.; Gorski, J.L.; Kurczynski, T.W.,1994

3. Two patients with 22ql3.3 deletions have similar facies and developmental patterns;Zwaigenbaum, L.; Siegel-Bartelt, J.; Teshima, I.; Ho, C.;Am J Hum Genet,1990

4. The ACT cytogenetics laboratory manual;Barch, M.J.,1990

5. Integration of physical, breakpoint and genetic maps of chromosome 22. Localization of 587 yeast artificial chromosomes with 238 mapped markers;Bell, C.J.; Budarf, M.L.; Nieuwenhuijsen, B.W.;Hum Mol Genet,1995

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